Chromoionophore I (ETH 5294) - BioReagent, for Microscopy, for Fluorescence analysis, ≥95%(HPLC), used for Chromoionophore I may be used for the test zone preparation in the multianalyte sensor, during environmental monitoring, using photographic digital

CAS: 125829-24-5 Cat. No.: C1454620 Formula: C₃₈H₅₃N₃O₂ Molecular Weight: 583.85 Beilstein Registry Number: 3576427 PubChem CID: 4403211

GRADE & PURITY BioReagent, for Fluorescence analysis, for Microscopy, ≥95%(HPLC)

Storage

Store at 2-8°C,Protected from light,Desiccated

Shipped In

Wet ice

Application

Calcium Ion Detection, Fluorescence Analysis

Overview

 Chromoionophore I (ETH 5294) is a H+-selective neutral chromoionophore, which is lipophilic in nature and is a highly basic dye molecule.

Application

Chromoionophore I may be used for the test zone preparation in the multianalyte sensor, during environmental monitoring, using photographic digital camera. 

Selected examples 

Assay of K⁺ and of Ca²⁺ activity with solvent polymeric optode membrane based on ETH 5294 and potassium ionophore I (valinomycin)

Specifications

Specifications & Purity

BioReagent, for Microscopy, for Fluorescence analysis, ≥95%(HPLC)

Application

Chromoionophore I may be used for the test zone preparation in the multianalyte sensor, during environmental monitoring, using photographic digital camera.

Stability And Storage

Store at 2-8℃ long term (12 months). Store in the dark. Desiccated.

Storage

Store at 2-8°C,Protected from light,Desiccated

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Grade

BioReagent, for Fluorescence analysis, for Microscopy

Purity

≥95%(HPLC)

Names and Identifiers

• Canonical Smiles: CCCCCCCCCCCCCCCCCC(=O)N=C1C=C2C(=NC3=C(O2)C=C(C=C3)N(CC)CC)C4=CC=CC=C41
• IUPAC Name: N-[9-(diethylamino)benzo[a]phenoxazin-5-ylidene]octadecanamide
• InChIKey: MYWBZQJIXVRCJC-UHFFFAOYSA-N
• INCHI: 1S/C38H53N3O2/c1-4-7-8-9-10-11-12-13-14-15-16-17-18-19-20-25-37(42)39-34-29-36-38(32-24-22-21-23-31(32)34)40-33-27-26-30(28-35(33)43-36)41(5-2)6-3/h21-24,26-29H,4-20,25H2,1-3H3
• Isomeric SMILES: CCCCCCCCCCCCCCCCCC(=O)N=C1C=C2C(=NC3=C(O2)C=C(C=C3)N(CC)CC)C4=CC=CC=C41
• PubChem CID: 4403211
• Molecular Weight: 583.85
• Beilstein: 3576427

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Benzoxazines
      • Subclass Phenoxazines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Benzoxazines
• Subclass: Phenoxazines
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenoxazines
• Alternative Parents: Naphthalenes Dialkylarylamines Secondary ketimines Heteroaromatic compounds N-acylimines Amino acids and derivatives Oxacyclic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Phenoxazine - Naphthalene - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Benzenoid - Secondary ketimine - Heteroaromatic compound - Amino acid or derivatives - Tertiary amine - N-acylimine - Carboxylic acid derivative - Oxacycle - Azacycle - Amine - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as phenoxazines. These are polycyclic aromatic compounds containing a phenoxazine moiety, which is a linear tricyclic system that consists of a two benzene rings joined by a 1,4-oxazine ring.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: Soluble in alcohols, chloroform, DMSO or DMF.
• Sensitivity: light sensitive